FDA
Betamethasone Dipropionate
The FDA lists this product in 48 strengths and forms.
Composition
- Active ingredients
- BETAMETHASONE DIPROPIONATE EQ 0.05% BASE
Strengths and forms
The FDA lists each strength of a product separately; these pages share one label.
- BETAMETHASONE DIPROPIONATE EQ 0.05% BASE · OintmentNDA019141-001 · Prescription
- BETAMETHASONE DIPROPIONATE EQ 0.05% BASE · CreamANDA219348-001 · Prescription
- BETAMETHASONE DIPROPIONATE EQ 0.05% BASE · LotionANDA070281-001 · Discontinued
- BETAMETHASONE DIPROPIONATE EQ 0.05% BASE · CreamANDA070885-001 · Prescription
- BETAMETHASONE DIPROPIONATE EQ 0.05% BASE · LotionANDA071085-001 · Discontinued
- BETAMETHASONE DIPROPIONATE EQ 0.05% BASE · LotionANDA071882-001 · Discontinued
- BETAMETHASONE DIPROPIONATE EQ 0.05% BASE · CreamANDA072536-001 · Discontinued
- BETAMETHASONE DIPROPIONATE EQ 0.05% BASE · Lotion, augmentedANDA077477-001 · Prescription
- BETAMETHASONE DIPROPIONATE EQ 0.05% BASE · Lotion, augmentedANDA077111-001 · Prescription
- BETAMETHASONE DIPROPIONATE EQ 0.05% BASE · CreamNDA019136-001 · Discontinued
At a glance
- Brand name
- Betamethasone Dipropionate
- Route
- Topical
- Dosage form
- Ointment
- Applicant
- Sun Pharma Canada
- Status
- Discontinued
- FDA approval
- 15 Sept 1994
- Application
- ANDA074271-001